A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276903



Internal ID20843943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92091586..92092750hg38UCSC Ensembl
chr7:91720900..91722064hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg381165
hg191165
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575079
Supporting Variants
Samples
Known GenesAKAP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276903
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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